A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891875



Internal ID18839585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82171786..82294496hg38UCSC Ensembl
Outerchr10:82171786..82294496hg38UCSC Ensembl
Innerchr10:83931542..84054252hg19UCSC Ensembl
Outerchr10:83931542..84054252hg19UCSC Ensembl
Innerchr10:83921522..84044232hg18UCSC Ensembl
Outerchr10:83921522..84044232hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38122711
hg19122711
hg18122711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780864
Samples
Known GenesNRG3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891875
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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